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About this Operator Manufacturing, Launch Operations role at Bristol Myers Squibb

Bristol Myers Squibb · Onsite · Boudry - CH
This job posting is in French.

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.


Mission principale:


L’Operator Manufacturing, Launch Operations aura pour mission d’assurer les activités de fabrication des produits essentiellement sous forme de comprimés ou capsules, dans le respect de la réglementation BPF / GMPs, des règles d’hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.


Responsabilités:


  • Réaliser des opérations de production tel que la pesée des matières, la préparation des mélanges de poudre ainsi que la conduite de ligne automatisée dans les activités de fabrication de comprimés ou capsules suivant son curriculum de formation et selon les procédures en vigueur du système qualité.
  • Maitriser l’outil MES (Manufacturing Execution System) dans la gestion des dossiers de lot et des consommations associées.
  • Maîtriser et effectuer le nettoyage des équipements du matériel et des salles liées aux différentes étapes de production.
  • Réaliser les changements de formats et réglages de base définis dans les procédures.
  • Effectuer les vides des lignes de production.
  • Effectuer les contrôles physiques élémentaire des produits fabriqués.
  • Se conformer aux objectifs de production notamment au respect du planning établi.
  • Assurer la réalisation des opérations de production des lots techniques, commerciaux et cliniques en environnement GMP et travailler de façon autonome et efficace selon les consignes de son responsable.
  • Participer aux transferts de nouveaux produits, à la validation des procédés industriels, à la fabrication des lots de validation et à la qualification deséquipements.
  • Contrôler, enregistrer et compléter les documents de travail préétablis pourassurer un suivi des opérations réalisées (dossiers de lots remplis selon lesBPF / GMP).
  • Se conformer aux règles de sécurité et de sureté du site pharmaceutique.
  • Annoncer les situations dangereuses, les presqu’accidents/incidents et les accidents qui pourraient survenir sur le site auprès de son responsable direct et auprès du département EHS (Environment, Health & Safety).
  • Cette description de poste n’est pas exhaustive ; d’autres tâches etresponsabilités peuvent être confiées en fonction des besoins del’entreprise.

Profil requis:


  • Avoir une formation initiale de niveau CFC et une expérience de 5 ans dans le domaine de l’industrie pharmaceutique ou équivalente.
  • Connaître l’environnement BPF / GMP.
  • Avoir une parfaite maîtrise du français.
  • Être organisé et rigoureux, et avoir des qualités relationnelles pour un travail d’équipe.
  • Avoir de bonnes connaissances de base de l’outil informatique. (Word, Excel, Power point, Outlook).
  • Savoir utiliser un MES.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.


Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/


Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.



R1607219 : Operator Manufacturing, Launch Operations
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About Bristol Myers Squibb

Data Privacy Link W e’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

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